Caroline Stuart

Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder

Robert Kleta, Elisa Romeo, Zorica Ristic et al. · Nature Genetics · 2004 · 309 citations · Full text

Life Sciences, Genetics, Molecular Genetics +6

Triple-A syndrome with prominent ophthalmic features and a novel mutation in the AAASgene: a case report

Brian P. Brooks, Robert Kleta, Rafael C. Caruso et al. · BMC Ophthalmology · 2004 · 59 citations · Full text

Medicine, Genetics, Ophthalmology +17

Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity

Chiara Fallerini, Nicola Picchiotti, Margherita Baldassarri et al. · Human Genetics · 2021 · 41 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Knowledge and management of sport-related concussion in primary care in New Zealand.

Caroline Stuart, Duncan Reid, Alice Theadom et al. · PubMed · 2022 · 10 citations

Medicine, Neurology, Health Assessment +9